What is NDC 63083-7301?

63083-7301 is the product NDC for First Chakra (Root) 7301 (first chakra (root)), Marsdenia cundurango whole 6 [hp_X]/29.5mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

First Chakra (Root) 7301 (First Chakra (Root)).

What is the active ingredient?

Marsdenia cundurango whole, Arnica montana whole, Helleborus niger root, Potassium phosphate, Unspecified form, Magnesium phosphate, Dibasic trihydrate, Sodium fluoride, Apis mellifera, Bos taurus bile, Lycosa tarantula, Ferric oxide red, Silicon dioxide.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for First Chakra (Root) 7301?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

First Chakra (Root) 7301 NDC 63083-7301

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7301Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7301Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63083-7301-1	6308373010163083730101	29.5 mL in 1 BOTTLE, DROPPER (63083-7301-1)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): First Chakra (Root) 7301Suffix: 7301
Generic name (nonproprietary): first chakra (root)
Active ingredients: Marsdenia cundurango whole — 6 [hp_X]/29.5mLArnica montana whole — 8 [hp_X]/29.5mLHelleborus niger root — 8 [hp_X]/29.5mLPotassium phosphate, Unspecified form — 8 [hp_X]/29.5mLMagnesium phosphate, Dibasic trihydrate — 8 [hp_X]/29.5mLSodium fluoride — 8 [hp_X]/29.5mLApis mellifera — 12 [hp_X]/29.5mLBos taurus bile — 12 [hp_X]/29.5mLLycosa tarantula — 12 [hp_X]/29.5mLFerric oxide red — 30 [hp_X]/29.5mLSilicon dioxide — 30 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-7301_10ab58f2-3d40-4b0b-b804-7a4a5ad00a4dSPL ID 10ab58f2-3d40-4b0b-b804-7a4a5ad00a4dSPL set ID 61eb1bbe-6675-4369-b852-18975e6b08c7UNII AT33ZFZ5A1, O80TY208ZW, 608DGJ6815, B7862WZ632, HF539G9L3Q, 8ZYQ1474W7, 7S82P3R43Z, ET3651ZLOU, 86M454L2TT, 1K09F3G675, ETJ7Z6XBU4
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Standardized Insect Venom Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083730101 followed by a unit qualifier and the quantity

Package 63083-7301-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS Temporarily relieves restlessness, insecurity, impatience, greediness, anger or aggression, or obsession with materialistic matters.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-7301

What is NDC 63083-7301?: 63083-7301 is the product NDC for First Chakra (Root) 7301 (first chakra (root)), Marsdenia cundurango whole 6 [hp_X]/29.5mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: First Chakra (Root) 7301 (First Chakra (Root)).
What is the active ingredient?: Marsdenia cundurango whole, Arnica montana whole, Helleborus niger root, Potassium phosphate, Unspecified form, Magnesium phosphate, Dibasic trihydrate, Sodium fluoride, Apis mellifera, Bos taurus bile, Lycosa tarantula, Ferric oxide red, Silicon dioxide.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for First Chakra (Root) 7301?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

First Chakra (Root) 7301 (First chakra (root)) NDC 63083-7301